论文部分内容阅读
在白塑料桶和水泥池中进行了雨生红球藻诱变株1号大量培养试验,温度为14~18.5℃,结果为:桶接种密度分别为8.1×103个/ml、6.5×103个/ml、6.6×103个/ml,经过12 d的培养,密度分别为14.7×104个/ml、14.3×104个/ml、14.7×104个/ml;水泥池接种密度分别为2.0×103个/ml、5.1×103个/ml、3.5×103个/ml,经过11 d的培养,密度分别为7.9×104个/ml、10.0×104个/ml、9.2×104个/ml。动细胞藻密度分别为8.2×104个/ml、14.7×104个/ml、22.4×104个/ml,收获到湿藻1616 g/m31、768 g/m32、488 g/m3,干藻86 g/m39、2 g/m31、32 g/m3;不动细胞藻密度分别为4.4×104个/ml、18.9×104个/ml,收获到湿藻1921 g/m3、4677 g/m3,干藻138 g/m3、342 g/m3。
In a white plastic bucket and a cement pool were conducted Haematococcus pluvialis mutagen No. 1, a large number of culture experiments, the temperature was 14 ~ 18.5 ℃, the results are: barrel inoculum density were 8.1 × 103 / ml, 6.5 × 103 / ml, 6.6 × 103 个 / ml, after 12 d of culture, the density was 14.7 × 104 个 / ml, 14.3 × 104 个 / ml, 14.7 × 104 个 / ml; the density of cement pool were 2.0 × 103 / ml, 5.1 × 103 / ml, 3.5 × 103 / ml, after 11 days of culture, the density was 7.9 × 104 cells / ml, 10.0 × 104 cells / ml, 9.2 × 104 cells / ml, respectively. The cell density of moving cells were 8.2 × 104 cells / ml, 14.7 × 104 cells / ml and 22.4 × 104 cells / ml respectively. The wet algae were 1616 g / m31, 768 g / m32, 488 g / m3 and 86 g / m39, 2 g / m31 and 32 g / m 3 respectively. The density of immobilized cells were 4.4 × 104 cells / ml and 18.9 × 104 cells / ml respectively. The dry algae were 1921 g / m3 and 4677 g / 138 g / m3, 342 g / m3.